Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

FDA drug recalls in 2015

Every FDA drug recall initiated in 2015, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

1,733 recalls, newest first.

Class III · Low risk

Norpace CR

Failed Dissolution Specification

Terminated Dissolution failure Pfizer Inc. NDC 0025-2742-31 D-0520-2016
Class II · Moderate risk

Oxygen

cGMP Deviations; trailer may not have met GMP requirements prior to filling

Terminated cGMP deviation AGA Gas Inc NDC 33237-001-01 D-0779-2016
Class I · High risk

SUPER HERBS 350 mg

Marketed without an approved NDA/ANDA - presence of undeclared sibutramine, desmethylsibutramine (an active metabolite of sibutramine) and/or phenolphthalein.

Terminated Chemical / undeclared Super Herbs D-0909-2016
Class III · Low risk

NABUMETONE Tablets USP

Labeling: Not Elsewhere Classified: Lack of leaflets and approved labels on bottles.

Terminated Labeling / mix-up Teva Pharmaceuticals USA D-0773-2016
Class II · Moderate risk

Dextroamphetamine Saccharate

Failed Impurities/Degradation Specifications: High out of specification test result for impurities during stability testing.

Terminated Impurity / degradation Teva Pharmaceuticals USA NDC 0555-0972-02 D-0566-2016
Class II · Moderate risk

tubby todd Bath Co

Microbial Contamination of Non-Sterile Products: Consumer complaint and subsequent testing found lot to be out of specification for mold.

Terminated Microbial contamination Mariposa Labs LLC D-0510-2019
Class II · Moderate risk

SyrSpend SF

Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF Grape Flavor are being recalled due to the presence of yeast.

Terminated Microbial contamination Fagron, Inc NDC 51552-1079-9 D-0656-2016
Class II · Moderate risk

SyrSpend SF

Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF Grape Flavor are being recalled due to the presence of yeast.

Terminated Microbial contamination Fagron, Inc NDC 51552-1167-9 D-0655-2016
Class II · Moderate risk

SyrSpend SF

Microbial Contamination of Non-Sterile Products: Syrspend SF and Syrspend SF Grape Flavor are being recalled due to the presence of yeast.

Terminated Microbial contamination Fagron, Inc NDC 51552-1079-5 D-0654-2016
Class II · Moderate risk

Rocuronium Bromide 50 MG/5ML INJ.

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 61786-0222-57 D-0517-2016
Class II · Moderate risk

Novolin 70/30

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 52125-0414-01 D-0516-2016
Class II · Moderate risk

Lorazepam 2 mg/mL Inj.

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 61786-0316-01 D-0515-2016
Class II · Moderate risk

Ascorbic Acid 500 MG/ML Inj.

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 61786-0431-16 D-0514-2016
Class II · Moderate risk

Vitamin B-Complex 100

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 52125-0873-02 D-0513-2016
Class II · Moderate risk

Bicillin L-A 600000 Units/mL Inj.

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 61786-0253-03 D-0512-2016
Class II · Moderate risk

Humulin 70/30

Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.

Terminated Labeling / mix-up RemedyRepack Inc. NDC 52125-0415-08 D-0511-2016

Recalls by year